Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.

Environmental stresses lower the efficiency of photosynthesis and sometimes cause irreversible damage to plant functions. When spinach thylakoids and Photosystem II membranes were illuminated with excessive visible light (100-1,000 µmol photons m(-1) s(-1)) for 10 min at either 20°C or 30°C, the opt...

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Main Authors: Tiffanie Chan, Yurika Shimizu, Pavel Pospíšil, Nobuyoshi Nijo, Anna Fujiwara, Yoshito Taninaka, Tomomi Ishikawa, Haruka Hori, Daisuke Nanba, Aya Imai, Noriko Morita, Miho Yoshioka-Nishimura, Yohei Izumi, Yoko Yamamoto, Hideki Kobayashi, Naoki Mizusawa, Hajime Wada, Yasusi Yamamoto
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3531424?pdf=render
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author Tiffanie Chan
Yurika Shimizu
Pavel Pospíšil
Nobuyoshi Nijo
Anna Fujiwara
Yoshito Taninaka
Tomomi Ishikawa
Haruka Hori
Daisuke Nanba
Aya Imai
Noriko Morita
Miho Yoshioka-Nishimura
Yohei Izumi
Yoko Yamamoto
Hideki Kobayashi
Naoki Mizusawa
Hajime Wada
Yasusi Yamamoto
author_facet Tiffanie Chan
Yurika Shimizu
Pavel Pospíšil
Nobuyoshi Nijo
Anna Fujiwara
Yoshito Taninaka
Tomomi Ishikawa
Haruka Hori
Daisuke Nanba
Aya Imai
Noriko Morita
Miho Yoshioka-Nishimura
Yohei Izumi
Yoko Yamamoto
Hideki Kobayashi
Naoki Mizusawa
Hajime Wada
Yasusi Yamamoto
author_sort Tiffanie Chan
collection DOAJ
description Environmental stresses lower the efficiency of photosynthesis and sometimes cause irreversible damage to plant functions. When spinach thylakoids and Photosystem II membranes were illuminated with excessive visible light (100-1,000 µmol photons m(-1) s(-1)) for 10 min at either 20°C or 30°C, the optimum quantum yield of Photosystem II decreased as the light intensity and temperature increased. Reactive oxygen species and endogenous cationic radicals produced through a photochemical reaction at and/or near the reaction center have been implicated in the damage to the D1 protein. Here we present evidence that lipid peroxidation induced by the illumination is involved in the damage to the D1 protein and the subunits of the light-harvesting complex of Photosystem II. This is reasoned from the results that considerable lipid peroxidation occurred in the thylakoids in the light, and that lipoxygenase externally added in the dark induced inhibition of Photosystem II activity in the thylakoids, production of singlet oxygen, which was monitored by electron paramagnetic resonance spin trapping, and damage to the D1 protein, in parallel with lipid peroxidation. Modification of the subunits of the light-harvesting complex of Photosystem II by malondialdehyde as well as oxidation of the subunits was also observed. We suggest that mainly singlet oxygen formed through lipid peroxidation under light stress participates in damaging the Photosystem II subunits.
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spelling doaj.art-a8ac6733084945d28a7baefa15569f8b2022-12-21T23:32:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5210010.1371/journal.pone.0052100Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.Tiffanie ChanYurika ShimizuPavel PospíšilNobuyoshi NijoAnna FujiwaraYoshito TaninakaTomomi IshikawaHaruka HoriDaisuke NanbaAya ImaiNoriko MoritaMiho Yoshioka-NishimuraYohei IzumiYoko YamamotoHideki KobayashiNaoki MizusawaHajime WadaYasusi YamamotoEnvironmental stresses lower the efficiency of photosynthesis and sometimes cause irreversible damage to plant functions. When spinach thylakoids and Photosystem II membranes were illuminated with excessive visible light (100-1,000 µmol photons m(-1) s(-1)) for 10 min at either 20°C or 30°C, the optimum quantum yield of Photosystem II decreased as the light intensity and temperature increased. Reactive oxygen species and endogenous cationic radicals produced through a photochemical reaction at and/or near the reaction center have been implicated in the damage to the D1 protein. Here we present evidence that lipid peroxidation induced by the illumination is involved in the damage to the D1 protein and the subunits of the light-harvesting complex of Photosystem II. This is reasoned from the results that considerable lipid peroxidation occurred in the thylakoids in the light, and that lipoxygenase externally added in the dark induced inhibition of Photosystem II activity in the thylakoids, production of singlet oxygen, which was monitored by electron paramagnetic resonance spin trapping, and damage to the D1 protein, in parallel with lipid peroxidation. Modification of the subunits of the light-harvesting complex of Photosystem II by malondialdehyde as well as oxidation of the subunits was also observed. We suggest that mainly singlet oxygen formed through lipid peroxidation under light stress participates in damaging the Photosystem II subunits.http://europepmc.org/articles/PMC3531424?pdf=render
spellingShingle Tiffanie Chan
Yurika Shimizu
Pavel Pospíšil
Nobuyoshi Nijo
Anna Fujiwara
Yoshito Taninaka
Tomomi Ishikawa
Haruka Hori
Daisuke Nanba
Aya Imai
Noriko Morita
Miho Yoshioka-Nishimura
Yohei Izumi
Yoko Yamamoto
Hideki Kobayashi
Naoki Mizusawa
Hajime Wada
Yasusi Yamamoto
Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
PLoS ONE
title Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
title_full Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
title_fullStr Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
title_full_unstemmed Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
title_short Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination.
title_sort quality control of photosystem ii lipid peroxidation accelerates photoinhibition under excessive illumination
url http://europepmc.org/articles/PMC3531424?pdf=render
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